Cited by 1,310Neuroinflammation and Neurodegeneration MechanismsSingle-cell and spatial transcriptomicsMultiple Sclerosis Research Studies

Spatial and temporal heterogeneity of mouse and human microglia at single-cell resolution

Open access
Masuda, Takahiro, Sankowski, Roman, Staszewski, Ori, Böttcher, Chotima, Amann, Lukas, Sagar, Scheiwe, Christian, Nessler, Stefan +11 more·2019·Nature

Abstract

Microglia have critical roles not only in neural development and homeostasis, but also in neurodegenerative and neuroinflammatory diseases of the central nervous system 1-4. These highly diverse and specialized functions may be executed by subsets of microglia that already exist in situ, or by specific subsets of microglia that develop from a homogeneous pool of cells on demand. However, little is known about the presence of spatially and temporally restricted subclasses of microglia in the central nervous system during development or disease. Here we combine massively parallel single-cell analysis, single-molecule fluorescence in situ hybridization, advanced immunohistochemistry and computational modelling to comprehensively characterize subclasses of microglia in multiple regions of the central nervous system during development and disease. Single-cell analysis of tissues of the central nervous system during homeostasis in mice revealed specific time- and region-dependent subtypes of microglia. Demyelinating and neurodegenerative diseases evoked context-dependent subtypes of microglia with distinct molecular hallmarks and diverse cellular kinetics. Corresponding clusters of microglia were also identified in healthy human brains, and the brains of patients with multiple sclerosis. Our data provide insights into the endogenous immune system of the central nervous system during development, homeostasis and disease, and may also provide new targets for the treatment of neurodegenerative and neuroinflammatory pathologies.

Integrity signals

Registry

Crossref · 10.1038/s41586-019-0924-x

Cites

37 of 37 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Masuda, T., Sankowski, R., Staszewski, O., Böttcher, C., Amann, L., Sagar, Scheiwe, C., Nessler, S., Kunz, P., van Loo, G., Coenen, V. A., Reinacher, P. C., Michel, A., Sure, U., Gold, R., Grün, D., Priller, J., Stadelmann, C., & Prinz, M.
Affiliations
  • University of Freiburg (DE)
  • Charité – Universitätsmedizin Berlin (DE)
  • Max Planck Institute of Immunobiology and Epigenetics (DE)
  • Universitätsmedizin Göttingen (DE)
  • Essen University Hospital (DE)
  • St. Josef-Hospital (DE)
  • German Center for Neurodegenerative Diseases (DE)
Corresponding author
Prinz, Marco
Venue
Nature
Published
2019-02
Volume
566
Issue
7744
Pages
388-392
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2914756534
Cited by
1,310
References
37
Citations by year
2026: 136 · 2025: 145 · 2024: 187 · 2023: 184 · 2022: 207 · 2021: 209 · 2020: 169 · 2019: 71 · 2017: 1 · 2012: 1
FWCI
72.26
Type
journal article
Language
en
Locations
  • Nature (publishedVersion)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
  • Ghent University Academic Bibliography (Ghent University) (submittedVersion)
  • DZNE Pub (submittedVersion)
  • GoeScholar The Publication Server of the Georg-August-Universität Göttingen (Georg-August-Universität Göttingen) (submittedVersion, cc-by)
  • Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
  • MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
Funders
  • National Multiple Sclerosis Society
  • Deutsche Forschungsgemeinschaft (SFB-1160, SFB 992, SFB/ TRR 167, TRR 167)
  • Bundesministerium für Bildung und Forschung
  • Karolinska Institutet
  • Deutschen Multiple Sklerose Gesellschaft
  • Kanae Foundation for the Promotion of Medical Science
  • Roman, Marga und Mareille Sobek Stiftung
  • Medical Research Council (MC_PC_16031)
  • Japan Society for the Promotion of Science
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
Keywords
microglia, microglial heterogeneity, microglial subtypes, central nervous system development, neuroinflammation, neurodegenerative diseases, demyelination, multiple sclerosis, mouse brain, human brain, single-cell transcriptomics, single-molecule fluorescence in situ hybridization, brain homeostasis
MeSH terms
Animals, Brain, Cell Separation, Demyelinating Diseases, Female, Humans, Kinetics, Male, Multiple Sclerosis, Case-Control Studies, Microglia, Neurodegenerative Diseases, Mice, Single-Cell Analysis, Spatio-Temporal Analysis

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review